FDA Inspection 812547 — Acorda Therapeutics, Inc.

Acorda Therapeutics, Inc. — FEI 3002457563

The FDA completed an inspection of Acorda Therapeutics, Inc. on December 7, 2012 in Pearl River, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 7, 2012
Fiscal Year
2013
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Pearl River, NY (United States)

Additional Details

Risk Evaluation and Mitigation Strategies (REMS)